1. Krüppel-like Factor-9 and Krüppel-like Factor-13: Highly Related, Multi-Functional, Transcriptional Repressors and Activators of Oncogenesis
   Frank A. Simmen et al, 2023, Cancers CrossRef
2. Genetic Risk Score Constructed from Polymorphisms in the VEGFA, TBX5, and SMAD7 Genes Provides Novel Insights into the Molecular Mechanisms of the Tetralogy of Fallot and Ventricular Septal Defect (Case-Control Study from the Pakistani Population)
   Sana Ashiq et al, 2023, The American Journal of Cardiology CrossRef
3. Somatic GATA4 mutation contributes to tetralogy of Fallot
   Pradhan Abhinav et al, 2024, Experimental and Therapeutic Medicine CrossRef
4. The Involvement of Krüppel-like Factors in Cardiovascular Diseases
   Michelle G. Santoyo-Suarez et al, 2023, Life CrossRef
5. The kruppel-like factor (KLF) family, diseases, and physiological events
   Kemal Yuce et al, 2024, Gene CrossRef
6. Identification and Functional Investigation of SOX4 as a Novel Gene Underpinning Familial Atrial Fibrillation
   Wei-Feng Jiang et al, 2024, Diagnostics CrossRef
7. A Comprehensive Review of Management Strategies for Bicuspid Aortic Valve (BAV): Exploring Epidemiology, Aetiology, Aortopathy, and Interventions in Light of Recent Guidelines
   Halil Ibrahim Bulut et al, 2023, Journal of Cardiovascular Development and Disease CrossRef
8. KLF13 promotes VSMCs phenotypic dedifferentiation by directly binding to the SM22α promoter
   Xiaofan Yuan et al, 2024, Journal of Cellular Physiology CrossRef
9. Discovery and functional investigation of BMP4 as a new causative gene for human congenital heart disease
   Zhi Wang, 2024, American Journal of Translational Research CrossRef
10. SMAD4 loss-of-function mutation predisposes to congenital heart disease
    Yin Wang et al, 2023, European Journal of Medical Genetics CrossRef
11. Discovery of BMP10 as a new gene underpinning congenital heart defects
    Bin-Bin Dong, 2024, American Journal of Translational Research CrossRef
12. Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease
    Hong-Yu Shi et al, 2022, Diagnostics CrossRef
13. Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias
    Yan-Jie Li et al, 2023, Biology CrossRef
14. Is the Cis-Element CACCC-Box a Master Regulatory Element during Cardiovascular Disease? A Bioinformatics Approach from the Perspective of the Krüppel-like Family of Transcription Factors
    Juan Andrés García-Loredo et al, 2024, Life CrossRef